Suppr超能文献

使用全基因组扩增技术对肌营养不良蛋白基因缺失进行植入前单细胞分析。

Preimplantation single cell analyses of dystrophin gene deletions using whole genome amplification.

作者信息

Kristjansson K, Chong S S, Van den Veyver I B, Subramanian S, Snabes M C, Hughes M R

机构信息

Institute for Molecular Genetics, Baylor College of Medicine, Houston, Texas 77030.

出版信息

Nat Genet. 1994 Jan;6(1):19-23. doi: 10.1038/ng0194-19.

Abstract

Primer extension preamplification (PEP) increases the scope and capacity of single cell genetic diagnosis by generating sufficient template to perform multiple subsequent DNA analyses using the polymerase chain reaction. We report the simultaneous analysis of single cells at five commonly deleted dystrophin exons and at the ZFX/ZFY loci. Ninety three percent of PEP reactions with single amniocytes, chorionic villus cells and blastomeres were successful, and a blinded analysis of single lymphoblasts from affected males resulted in 93% diagnostic accuracy, demonstrating its applicability in preimplantation prevention of Duchenne muscular dystrophy. Transfer of unaffected male embryos and improved diagnostic reliability are achieved with the ability to perform replicate multilocus analyses from the same blastomere.

摘要

引物延伸预扩增(PEP)通过生成足够的模板以利用聚合酶链反应进行多个后续DNA分析,从而扩大了单细胞基因诊断的范围并提高了其能力。我们报告了对五个常见缺失的肌营养不良蛋白外显子以及ZFX/ZFY基因座处的单细胞进行同步分析。对单个羊水细胞、绒毛膜绒毛细胞和卵裂球进行的PEP反应中,93%取得成功,对患病男性的单个淋巴细胞进行的盲法分析诊断准确率达93%,证明了其在杜氏肌营养不良症植入前预防中的适用性。通过能够对同一卵裂球进行重复多位点分析,实现了未受影响男性胚胎的移植并提高了诊断可靠性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验